Overview

The Mattheyses laboratory is interested in how cells interact with each other and their environment, and how the spatial-temporal dynamics and regulation of this communication directly impacts cellular homeostasis and function. We develop and apply innovative fluorescence microscopy techniques to elucidate the dynamics, forces, and organization of proteins within macromolecular assemblies central to cellular communication. Our three main areas of interest are: the organization and regulation of desmosomes, mechano-transduction and molecular forces in cell adhesion, and the spatio-temporal dynamics of endocytosis. Characteristics of proteins in the cellular environment – localization dynamics, higher-order organization and assembly, and mechanical tension – can alter function, yet the number of tools that can dissect the native physical environment of proteins lags behind that of biochemical analyses. Our research combines sophisticated imaging including super-resolution fluorescence microscopy (SIM and STORM), total internal reflection fluorescence (TIRF), fluorescence polarization, and microscopy technique development with primary and continuous cell culture models, molecular biology, theoretical modeling, and image analysis.  Our goal is to gain a mechanistic understanding of the dynamics and function of macromolecular complexes in cellular communication and providing insight into the cellular basis for human health and disease. 

Nanoscale Structure and Function of Desmosomes

Center on Probes for Molecular Mechanotechnology

The goal of our NIH funded center is to develop and optimize technologies to enable the study of mechanobiology and mechanotransduction pathways in living cells. The CPMM includes three highly synergistic Technology Development Projects that will be led by Alexa Mattheyses, Khalid Salaita (Emory), and Yonggang Ke (Emory).

TDP #1 (Mattheyses lead) High Resolution Mechanobiology